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Sotalol hydrochloride

CAS No.
959-24-0
Chemical Name:
Sotalol hydrochloride
Synonyms
SOTALOL HCL;DAROB;SOTALEX;SOTACOR;MJ-1999;BETAPACE;DL-MJ 1999;SOLATOL HCL;Betapace AF;meadjohnson1999
CBNumber:
CB9712098
Molecular Formula:
C12H20N2O3S.ClH
Molecular Weight:
308.83
MDL Number:
MFCD00242937
MOL File:
959-24-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:50:28

Sotalol hydrochloride Properties

Melting point 218-220°C
storage temp. 2-8°C
solubility H2O: 20 mg/mL
form powder
color white to off-white
Water Solubility Soluble in phosphate buffered saline, DMSO, ethanol, water, and methanol.
Major Application pharmaceutical small molecule
InChI InChI=1S/C12H20N2O3S.ClH/c1-9(2)13-8-12(15)10-4-6-11(7-5-10)14-18(3,16)17;/h4-7,9,12-15H,8H2,1-3H3;1H
InChIKey VIDRYROWYFWGSY-UHFFFAOYSA-N
SMILES C(C1C=CC(=CC=1)NS(=O)(=O)C)(O)CNC(C)C.Cl
CAS DataBase Reference 959-24-0(CAS DataBase Reference)
FDA UNII HEC37C70XX
UNSPSC Code 41116107
NACRES NA.24

Pharmacokinetic data

Excreted unchanged in urine >90%
Volume of distribution 1.6-2.4(L/kg)
Biological half-life 10-20 / 56

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H303-H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P405-P501a-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  PB0826000
HS Code  2935904000
Storage Class 11 - Combustible Solids
Toxicity LD50 in male mice, rats (mg/kg): 2600, 3450 orally; 670, 680 i.p.; LD50 orally in rabbits: 1000 mg/kg; LD50 i.p. in dogs: 330 mg/kg (Lish)

Sotalol hydrochloride price More Price(71)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000114 Sotalol hydrochloride European Pharmacopoeia (EP) Reference Standard 25 mg $241 2026-04-30 Buy
Sigma-Aldrich PHR2798 Sotalol Hydrochloride 959-24-0 500MG $335 2026-04-30 Buy
Sigma-Aldrich 1617408 Sotalol hydrochloride United States Pharmacopeia (USP) Reference Standard 959-24-0 300mg $538 2026-04-30 Buy
Sigma-Aldrich 39863 (±)-Sotalol hydrochloride analytical standard 959-24-0 10mg $144 2022-05-15 Buy
Cayman Chemical 16136 Sotalol (hydrochloride) ≥98% 959-24-0 10mg $36 2026-04-30 Buy
Product number Packaging Price Buy
Y0000114 25 mg $241 Buy
PHR2798 500MG $335 Buy
1617408 300mg $538 Buy
39863 10mg $144 Buy
16136 10mg $36 Buy

Sotalol hydrochloride Chemical Properties, Uses, Production

Description

Sotalol is a non-selective antagonist of β-adrenergic receptors (β-ARs; IC50s = 8.9 and 5.2 μM for β1- and β2-ARs, respectively) and a class III antiarrhythmic agent. It decreases delayed outward potassium currents (IK) in guinea pig ventricular cells and prolongs action potential duration in electrically stimulated isolated guinea pig papillary muscles when used at a concentration of 100 μM. Sotalol decreases heart rate and increases blood pressure and the cardiac functional refractory period (FRP) in a canine model of ventricular tachycardia induced by programmed electrical stimulation (PES). Formulations containing sotalol have been used in the treatment of ventricular arrhythmias and maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL).

Description

Sotalol (hydrochloride) (Item No. 26291) is an analytical reference standard categorized as a β-adrenergic receptor antagonist. It has been detected as an adverse analytical finding (AAF) during anti-doping testing. This product is intended for use in analytical forensic applications. This product is also available as a general research tool .

Chemical Properties

White Crystalline Solid

Originator

Sotagard,Glaxo

Uses

Sotalol hydrochloride is used as a potent beta adrenergic antagonist, prolongs the action potential and increases the refractory period. Sotalol hydrochloride is also considered a non-selective β blocker and a potassium channel blocker with an IC50 of 43 μM.

Uses

A potent -adrenergic receptor antagonist. A class III antiarrythmic. It has been shown to prolong action potential and increases the refractory period

Uses

A potent α-adrenergic receptor antagonist. A class III antiarrythmic. It has been shown to prolong action potential and increases the refractory period.

Uses

antibacterial

Definition

ChEBI: A hydrochloride salt that is the monohydrochloride of sotalol. It has both beta-adrenoreceptor blocking (Vaughan Williams Class II) and cardiac action potential duration prolongation (Vaughan Williams Class III) antiarrhythmic properties. It is used (usually as the hydrochloride salt) for the management of ventricular and supraventricular arrhythmias.

Manufacturing Process

As a resulting of reaction of methansulfonylchloride reacted with aniline methansulfonanilide was obtained. The methansulfonanilide reacted with bromacetylbromide at the presence of AlCl3 and CS2 and 4-(bromacetyl)- methansulfonanilide was prepeared.
Then to the 4-(bromacetyl)-methansulfonanilide isopropylamine was added to give 4-(1-oxo-2-isopropylaminoethyl)methansulfonanilide.The 4-(1-oxo-2-isopropylaminoethyl)methansulfonanilide was reduced by hydrogenesation in the presence of Pd-C catalyst and sodium borohydride. So 4-(1-hydroxy-2-isopropylaminoethyl)methansulfonanilide was obtained.
The 4-(1-hydroxy-2-isopropylaminoethyl)methansulfonanilide hydrochloride may be prepared by treatment of base with hydrochloric acid.

brand name

Betapace(Berlex); Sorine (Upsher Smith).

Therapeutic Function

Beta-adrenergic blocker, Antiarrhythmic

Biological Activity

A relatively potent pure β adrenergic antagonist, unique in possessing additional class III antiarrhythmic activity. Also available as part of the Mixed Adrenergic Tocriset™ .

Clinical Use

Beta-adrenoceptor blocker:
Treatment of life-threatening ventricular arrhythmias
Prophylaxis of SVT

Veterinary Drugs and Treatments

Sotalol may be useful in the treatment of ventricular tachycardias and, possibly, supraventricular tachycardias in dogs.

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Analgesics: NSAIDs antagonise hypotensive effect.
Anti-arrhythmics: increased risk of myocardial depression and bradycardia; increased risk ofbradycardia, myocardial depression and AV block with amiodarone; increased risk of ventricular arrhythmias with amiodarone, dronedarone, disopyramide or procainamide - avoid; increased risk of myocardial depression and bradycardia with flecainide.
Antibacterials: increased risk of ventricular arrhythmias with moxifloxacin - avoid; increased risk of ventricular arrhythmias with delamanid.
Antidepressants: enhanced hypotensive effect with MAOIs; increased risk of ventricular arrhythmias with tricyclics; increased risk of ventricular arrhythmias with citalopram, escitalopram and venlafaxine - avoid.
Antihistamines: increased risk of ventricular arrhythmias with mizolastine - avoid.
Antihypertensives: enhanced hypotensive effect; increased risk of withdrawal hypertension with clonidine; increased risk of first dose hypotensive effect with post-synaptic alpha-blockers such as prazosin.
Antimalarials: increased risk of bradycardia with mefloquine; avoid with artemether and lumefantrine and piperaquine with artenimol - increased risk of ventricular arrhythmias.
Antimuscarinics: increased risk of ventricular arrhythmias with tolterodine.
Antipsychotics: enhanced hypotensive effect with phenothiazines; increased risk of ventricular arrhythmias with amisulpride, droperidol, haloperidol, phenothiazines, pimozide, risperidone, sulpiride or zuclopenthixol - avoid with droperidol and zuclopenthixol.
Antivirals: increased risk of ventricular arrhythmias with saquinavir or telaprevir - avoid.
Atomoxetine: increased risk of ventricular arrhythmias.
Calcium-channel blockers: increased risk of bradycardia and AV block with diltiazem; hypotension and heart failure possible with nifedipine and nisoldipine; asystole, severe hypotension and heart failure with verapamil.
Cytotoxics: possible increased risk of bradycardia with crizotinib; increased risk of ventricular arrhythmias with vandetanib - avoid; increased risk of ventricular arrhythmias with arsenic trioxide, bosutinib, ceritinib, panobinostat and vandetanib.
Diuretics: enhanced hypotensive effect; increased risk of ventricular arrhythmias due to hypokalaemia.
Fingolimod: possibly increased risk of bradycardia.
Ivabradine: increased risk of ventricular arrhythmias.
Moxisylyte: possible severe postural hypotension. Ranolazine: avoid concomitant use.
Sympathomimetics: severe hypertension with adrenaline and noradrenaline and possibly with dobutamine.

Metabolism

Metabolism of sotalol is negligible, and it is excreted unchanged in the urine.

storage

Store at RT

References

[1] H. TSUCHIHASHI. Characteristics of 125I-iodocyanopindolol binding to β-adrenergic and serotonin-1B receptors of rat brain: selectivity of β-adrenergic agents[J]. European journal of pharmacology, 1990, 183 1: 404. DOI: 10.1016/0014-2999(90)93286-y

Sotalol hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 278)
Supplier Tel Email Country ProdList Advantage
Shandong Luoxin Pharmaceutical Co., Ltd. -- trade@luoxingroup.com China 33 60
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Jia Xing Isenchem Co.,Ltd 0573-85285100 18627885956 isenchem@163.com China 9389 66
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
Syntechem Co.,Ltd info@syntechem.com China 12973 57
Shanghai Aobo pharmaceutical Technology Co., Ltd 86-21-51320499 aobo@aobopharm.com China 297 57
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9791 79
Shanghai civi chemical technology co.,Ltd 86-21-34053660 sale@labgogo.com China 9853 52
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12323 58
NCE Biomedical Co.,Ltd. 4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988 China 1490 55

View Latest Price from Sotalol hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sotalol hydrochloride pictures 2026-09-02 Sotalol hydrochloride
959-24-0
$1.30-32.00 1KG 99% Henan Fengda Chemical Co., Ltd
Sotalol hydrochloride pictures 2021-07-13 Sotalol hydrochloride
959-24-0
$10.00-15.00 1KG 99%+ HPLC Zhuozhou Wenxi import and Export Co., Ltd
Sotalol hydrochloride pictures 2021-07-09 Sotalol hydrochloride
959-24-0
$10.00-15.00 1KG 99%+ HPLC Zhuozhou Wenxi import and Export Co., Ltd

Sotalol hydrochloride Spectrum

4-(2-isopropylamino-1-hydroxyaethyl)methanesulfonailidhydrochlorid 4’-(1-hydroxy-2-(isopropylamino)ethyl)methanesulfonanilidemonohydrochloride 4’-(1-hydroxy-2-(isopropylamino)ethyl)-methanesulfonanilidmonohydrochlorid isopropylaminohydroxyethylmethanesulfonanilidehydrochloride meadjohnson1999 n-isopropyl-beta-(4-methanesulfonamidophenyl)ethanolaminehydrochloride SOTACOR SOTALEX (+/-)-SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE MJ-1999 N-[4-[1-HYDROXY-2-[(1-METHYLETHYL)AMINO]ETHYL]PHENYL]METHANESULFONAMIDE HYDROCHLORIDE N-[4-(1-HYDROXY-2-[ISOPROPYLAMINO]ETHYL)-PHENYL]METHANESULFONAMIDE HYDROCHLORIDE D,L-Sotalol, Hydrochloride MJ-1999, Betapace, Darob, Sotacor, Sotalex 4'-[1-Hydroxy-2-(isopropylamino)ethyl]methanesulfonanilide hydrochloride 4'-[2-(Isopropylamino)-1-hydroxyethyl]methanesulfonanilide monohydrochloride DL-MJ 1999 Methanesulfonamide, N-[4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]-, monohydrochloride (9CI) N-Isopropyl-b-(4-methanesulfonamidophenyl)ethanolamine hydrochloride METHANESULPHONANILIDE41HYDROXY2ISOPROPYLAMINOETHYLMONOHYDROCHLORIDE 4'-(1-hydroxy-2-isopropylaminoethyl)methanesulphonanilide hydrochloride BETAPACE DAROB SOLATOL HCL (-N-[4-[1-Hydroxy-2-[(1-Methyl Ethyl) Amino]-ethyl]phenyl]methanesulfonamide SOTALOL HYDROCHLORIDE BP N-4-[1-Hydroxy-2-(isopropylamino)ethyl]methane sulfonanilide hydrochloride Beta-cardone hydrochloride Sotalol Hydrochloride (300 mg) Sotalol hydrochlorid Sotalol (Betapace) Sotalol hydrochloride COS Berlex Laboratories Betapace AF (±)-Sotalol hydrochloride,N-[4-[1-Hydroxy-2-(isopropylamino)ethyl]phenyl]methanesulfonamide hydrochloride MethanesulfonaMide,N-[4-[1-hydroxy-2-[(1-Methylethyl)aMino]ethyl]phenyl]-, hydrochloride (1:1) N-[4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]-methanesulfonamide,hydrochloride (1:1) Sotalol hydrochloride CRS N-[4-[(1RS)-1-Hydroxy-2-[(1-methylethyl)amino]ethyl]- phenyl]methanesulfonamide hydrochloride (+)-sotalol hydrochloride Sotalol hydrochloride USP/EP/BP Sotalol HCl (MJ 1999) Sotalol HydrochlorideQ: What is Sotalol Hydrochloride Q: What is the CAS Number of Sotalol Hydrochloride Q: What is the storage condition of Sotalol Hydrochloride Q: What are the applications of Sotalol Hydrochloride Sotalol Hydrochloride (1617408) Sotalol hydrochloride in methanol C16972630 SotaloLhydrochloride Sotalol HCl - Bio-X ? Sotalol hydrochloride 100 μg/mL in Acetonitrile Sotalol Hydrochloride 1.0 mg/ml in Methanol (as free base) SOTALOL HCL 959-24-0 C21H21ClN2O3S C12H20N2O3SxHCl C12H20N2O3SClH C12H21ClN2O3S C12H20N2O3SHCl EXCENEL